The Recall Desk

Manufacturer

Perrigo Company PLC

106 recalls in our database name Perrigo Company PLC as the manufacturing or recalling firm.

What the numbers show

Total
106
Critical
0
Severe
18
Most recent
2022-03-02

Of the 106 recalls from Perrigo Company PLC we have scored against our rubric, 0 (0%) are Critical — deaths or serious injuries reported, or the agency’s own highest classification — and 18 (17%) are Severe.

Which agencies issued them

About this listing

The manufacturer string comes from the agency’s own source notice — for FDA recalls, the “recalling firm” field; for NHTSA recalls, the vehicle manufacturer; for CPSC recalls, the firm-of-record on the joint press release. A single corporate family can appear under multiple manufacturer strings as agency notices aren’t standardized on a canonical name. If you don’t see recalls you expect, try a parent-company search or a broader full-text search.

Severity scores below are computed from the agency’s classification and the recall text, never from manufacturer behaviour or history. Many manufacturers issue routine corrective actions (software updates, labelling corrections) that are correctly scored low — having recalls on this list isn’t inherently a quality signal.

101–106 of 106

  • HighFDA (Food)·F-1155-2019·2019-03-20

    Perrigo Recalls Simple Truth Organic Fruit Puree Pouches for Milk Labeling Error

    Perrigo is voluntarily recalling Simple Truth Organic Fruit Puree pouches because the packaging fails to declare the presence of milk.

    Product
    Simple Truth Organic Banana, Strawberry & Apple Fruit Puree with Nonfat Greek Yogurt, 113 g, packed in a laminate pouch, Each case has 6 cartons with 6 pouches per carton. Total of 36 pouches per case.
    Category
    Food
    Distribution
    16 states
  • ModerateFDA (Drugs)·D-0652-2016·2016-02-10

    Perrigo Recalls Nystatin Powder for Labeling Error on Declared Strength

    Perrigo is recalling 918 units of Nystatin USP Powder due to a labeling error regarding the declared strength. The product was distributed nationwide.

    Product
    Nystatin, USP Powder for Rx compounding, 150 Million Units, Packaged by Perrigo, Minneapolis MN 55427, NDC 0574-0404-15, UPC 305740404157
    Category
    Drug
    Distribution
    Distributed nationwide
  • ModerateFDA (Drugs)·D-0651-2016·2016-02-10

    Perrigo Recalls Nystatin Powder for Labeling Error on Declared Strength

    Perrigo Company PLC is recalling Nystatin, USP Powder for Rx compounding due to a labeling error regarding the declared strength.

    Product
    Nystatin, USP Powder for Rx compounding, 50 Million Units, Packaged by Perrigo, Minneapolis MN 55427, NDC 0574-0405-05, UPC 305740404058.
    Category
    Drug
    Distribution
    Distributed nationwide
  • ModerateFDA (Drugs)·D-0587-2016·2016-02-03

    Perrigo Recalls Children's Guaifenesin DM Liquid Due to Dosing Cup Errors

    Perrigo is recalling specific lots of Children's Guaifenesin DM Cherry liquid because the included dosing cups have incorrect dose markings.

    Product
    Guaifenesin DM Cherry liquid (guaifenesin 100 mg/5 mL and Dextromethorphan HBr 5 mg/5 mL), packaged in 4oz. bottles, co-packaged with a dosing cup in a carton and sold under the following: a) Sunmark, Children's Mucus Relief Cough, Guaifenesin 100 mg/Expectorant…
    Category
    Drug
    Distribution
    Distributed nationwide
  • ModerateFDA (Drugs)·D-0586-2016·2016-02-03

    Perrigo Recalls Guaifenesin Liquid Due to Incorrect Dosing Cup Markings

    Perrigo Company PLC is recalling specific lots of Guaifenesin liquid because the included dosing cups have incorrect dose markings.

    Product
    Guaifenesin Grape liquid 100 mg/5 mL, packaged in 4oz. bottles, co-packaged with a dosing cup in a carton and sold under the following: a) H.E.B. Mucus Relief, Children's Guaifenesin, Expectorant, Age 4+, Grape Flavor, Gluten Free, Alcohol Free, 4 FL OZ (118 mL) Bottle, Made…
    Category
    Drug
    Distribution
    Distributed nationwide
  • ModerateFDA (Drugs)·D-0525-2016·2015-12-30

    Perrigo Recalls Equaline All Day Allergy Tablets Due to Impurity

    Perrigo is recalling Equaline All Day Allergy tablets because they contain an impurity called cetirizine monosaccharide ester.

    Product
    EQUALINE ALL DAY ALLERGY — EQUALINE ALL DAY ALLERGY (CETIRIZINE HYDROCHLORIDE)
    Category
    Drug
    Distribution
    Distributed nationwide

About this company

Community-sourced company facts from Wikidata, not from any recall agency. This is background on the corporate entity — it says nothing about the recall(s) listed on this page, which come from the agency source notice above.

Perrigo Company Plc

pharmaceutical company

Country
Ireland
Founded
1887

Official website

Source: Wikidata (Q2916497), licensed CC0. Wikidata is community-edited and may not reflect the current corporate structure.